Retrospective analysis of the efficacy and tolerability of levetiracetam in brain tumor patients

被引:80
作者
Newton, Herbert B.
Goldlust, Samuel A.
Pearl, Dennis
机构
[1] Ohio State Univ, Med Ctr, Dardinger Neurooncol Ctr, Columbus, OH 43210 USA
[2] Ohio State Univ, Med Ctr, Div Neurooncol, Dept Neurol, Columbus, OH 43210 USA
[3] James Canc Hosp, Sch Med & Publ Hlth, Columbus, OH USA
[4] Solove Res Inst, Columbus, OH USA
[5] Ohio State Univ, Med Ctr, Dept Stat, Columbus, OH 43210 USA
关键词
anti-epileptic; brain tumor; keppra; levetiracetam; seizure;
D O I
10.1007/s11060-005-9070-4
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Seizures are a common complication of primary (PBT) and metastatic (MBT) brain tumors, affecting approximately 50% of all patients during the course of their illness. Anti-convulsant therapy of these tumor-induced seizures is often inadequate with conventional anti-epileptic drugs (AEDs), due to a variety of factors, including activation of glutaminergic NMDA receptors, immune-mediated neuronal damage, and anatomic alterations of neuronal input pathways. Levetiracetam (LEV) is a new AED with a novel mechanism of action, which includes reducing the Ca+ + current through neuron-specific, high voltage activated Ca+ + channels (n-type). Because of this unique mechanism, it has been postulated that LEV may be effective in controlling tumor-induced seizures. A retrospective chart review was performed of all patients who had received LEV for seizure control. Forty-one patients were reviewed (22 female, 19 male), with a median age of 47.5 years (range 25-81). There were 34 patients with PBT and 7 with MBT. LEV was used as an add-on AED in 33 patients and as monotherapy in eight patients, with a median dose of 1500 mg/day (range 500-3500). The baseline median seizure frequency for the cohort was 1 per week. After the addition of LEV and follow-up for a minimum of 4 weeks, the median seizure frequency was reduced to 0 per week (59% of patients noted complete seizure control). Overall, the seizure frequency was reduced in 90% of patients (P < 0.0001; Sign test). The most common toxicity was somnolence, noted in 37% of patients. LEV was very effective and well tolerated in brain tumor patients with seizures, and should be considered for add-on therapy to current AEDs, or as a substitute anti-convulsant for monotherapy.
引用
收藏
页码:99 / 102
页数:4
相关论文
共 24 条
[1]   Clinical experience of levetiracetam monotherapy for adults with epilepsy: 1-year follow-up study [J].
Alsaadi, TM ;
Shatzel, A ;
Marquez, AV ;
Jorgensen, J ;
Farias, S .
SEIZURE-EUROPEAN JOURNAL OF EPILEPSY, 2005, 14 (02) :139-142
[2]  
Bromfield Edward B, 2004, Rev Neurol Dis, V1 Suppl 1, pS27
[3]  
Elisevich K, 1999, PRACTICAL MANAGEMENT OF LOW-GRADE PRIMARY BRAIN TUMORS, P149
[4]   Preirradiation paclitaxel in glioblastoma multiforme: Efficacy, pharmacology, and drug interactions [J].
Fetell, MR ;
Grossman, SA ;
Fisher, JD ;
Erlanger, B ;
Rowinsky, E ;
Stockel, J ;
Piantadosi, S .
JOURNAL OF CLINICAL ONCOLOGY, 1997, 15 (09) :3121-3128
[5]   Efficacy and tolerability of the new antiepileptic drugs I: Treatment of new onset epilepsy - Report of the Therapeutics and Technology Assessment Subcommittee and Quality Standards Subcommittee of the American Academy of Neurology and the American Epilepsy Society [J].
French, JA ;
Kanner, AM ;
Bautista, J ;
Abou-Khalil, B ;
Browne, T ;
Harden, CL ;
Theodore, WH ;
Bazil, C ;
Stern, J ;
Schachter, SC ;
Bergen, D ;
Hirtz, D ;
Montouris, GD ;
Nespeca, M ;
Gidal, B ;
Marks, WJ ;
Turk, WR ;
Fischer, JH ;
Bourgeois, B ;
Wilner, A ;
Faught, RE ;
Sachdeo, RC ;
Beydoun, A ;
Glauser, TA .
NEUROLOGY, 2004, 62 (08) :1252-1260
[6]  
French JA, 2004, NEUROLOGY, V62, P1261, DOI 10.1212/01.WNL.0000123695.22623.32
[7]  
Habetswallner F, 2005, EUR J NEUROL, V12, P121
[8]   The role of human cytochrome P450 enzymes in the metabolism of anticancer agents: Implications for drug interactions [J].
Kivisto, KT ;
Kroemer, HK ;
Eichelbaum, M .
BRITISH JOURNAL OF CLINICAL PHARMACOLOGY, 1995, 40 (06) :523-530
[9]   Selective blockade of N-type calcium channels by levetiracetam [J].
Lukyanetz, EA ;
Shkryl, VM ;
Kostyuk, PG .
EPILEPSIA, 2002, 43 (01) :9-18
[10]   The synaptic vesicle protein SV2A is the binding site for the antiepileptic drug levetiracetam [J].
Lynch, BA ;
Lambeng, N ;
Nocka, K ;
Kensel-Hammes, P ;
Bajjalieh, SM ;
Matagne, A ;
Fuks, B .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2004, 101 (26) :9861-9866